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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129683Generated: October 25, 2026

N-methyl-N-phenethyl-2-[5-benzyloxy-3-(2-carbethoxyvinyl)indol-1-yl]acetamide → N-methyl-N-phenethyl-2-[5-benzyloxy-3-(4-carboxy-1,3-butadienyl)indol-1-yl]acetamide

https://huagongshe.com/reaction/129683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-N-phenethyl-2-[5-benzyloxy-3-(2-carbethoxyvinyl)indol-1-yl]acetamideHCID 53736924—
ReactantN-methyl-N-phenethyl-2-[5-benzyloxy-3-(2-carboxy-1,3-butadienyl)indol-1-yl]acetamideHCID 53760680—
ReactantN-methyl-N-phenethyl-2-[1-benzyloxy-3-(2-carbethoxy-2-methylvinyl)indol-5-yl]acetamideHCID 54354901—
SolventAcetone diethyletherHCID 21584533—
ProductN-methyl-N-phenethyl-2-[5-benzyloxy-3-(4-carboxy-1,3-butadienyl)indol-1-yl]acetamideHCID 53773500—

Reaction Steps

When N-methyl-N-phenethyl-2-[5-benzyloxy-3-(2-carboethoxyvinyl)-indol-1-yl]acetamide in the procedure of Example 23 is replaced with N-methyl-N-phenethyl-2-[1-benzyloxy-3-(2-carbethoxy-2-methylvinyl)indol-5-yl]acetamide then the product prepared is N-methyl-N-phenethyl-2-[5-benzyloxy-3-(2-carboxy-1,3-butadienyl)indol-1-yl]acetamide. (solvent system (acetone/ether) m.p. 189°-190° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468898
Source datasetuspto-grants-1995_11
ORD IDord-bd45b897922d43b99bb2b0c2e44457dd
Source noteuspto-grants-1995_11